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首页> 外文期刊>Molecular and Cellular Biology >Stable variant-specific transcripts of the variant cell surface glycoprotein gene 1.8 expression site in Trypanosoma brucei.
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Stable variant-specific transcripts of the variant cell surface glycoprotein gene 1.8 expression site in Trypanosoma brucei.

机译:布氏锥虫中变体细胞表面糖蛋白基因1.8表达位点的稳定变体特异性转录本。

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The structure and transcriptional regulation of the 1.8 variant cell surface glycoprotein (VSG) gene expression site located on a 430-kilobase (kb) chromosome was examined in a 430-kb-chromosome-specific library. Using 32P-labeled nascent transcripts generated by nuclear run-on, we selected recombinant clones derived from the 430-kb chromosome which were coordinately activated with the 1.8 VSG gene. The results show that a repetitive region with a minimum size of 27 kb is coordinately activated with the 1.8 VSG gene. As with the 1.8 VSG gene, transcription is by RNA polymerases that are insensitive to the drug alpha-amanitin at concentrations up to 1 mg/ml. Transcription results in the generation of several stable variant-specific mRNAs. These mRNAs most likely belong to a family of repetitive expression-site-associated genes.
机译:在430kb染色体特异性文库中检查了位于430千碱基(kb)染色体上的1.8个变体细胞表面糖蛋白(VSG)基因表达位点的结构和转录调控。利用核运行产生的32P标记的新生转录本,我们选择了由430-kb染色体衍生的重组克隆,这些克隆被1.8 VSG基因协同激活。结果表明,最小大小为27 kb的重复区被1.8 VSG基因协同激活。与1.8 VSG基因一样,转录是通过对浓度不超过1 mg / ml的药物α-amanitin不敏感的RNA聚合酶进行的。转录导致产生几种稳定的变体特异性mRNA。这些mRNA最有可能属于重复表达位点相关基因家族。

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